ID

24088

Descripción

Multicentre Study to Determine the Cardiotoxicity of R-CHOP Compared to R-COMP in Patients With Diffuse Large B-Cell Lymphoma; ODM derived from: https://clinicaltrials.gov/show/NCT00575406

Link

https://clinicaltrials.gov/show/NCT00575406

Palabras clave

Versiones (1)
  1. 25/7/17 25/7/17 -
Subido en

25 de julio de 2017

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Diffuse Large B-Cell Lymphoma NCT00575406

Inglés

Eligibility Diffuse Large B-Cell Lymphoma NCT00575406

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically confirmed, cd20 positive, diffuse large b-cell lymphoma (dlcl)
Descripción

Diffuse Large B-Cell Lymphoma CD20 antigen positive

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0079744
UMLS CUI [1,2]
C3888518
measurable disease according to international criteria
Descripción

Measurable Disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1513041
male or female
Descripción

Gender

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0079399
age 18 years and above
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
written informed consent
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
myocardial infarction within 6 months prior to study entry
Descripción

Myocardial Infarction

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0027051
cardiac insufficiency nyha grade 3 or 4
Descripción

Heart failure New York Heart Association Classification

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C1275491
previous treatment with chemotherapy or radiotherapy
Descripción

Chemotherapy | Therapeutic radiology procedure

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0392920
UMLS CUI [2]
C1522449
cns involvement of the disease
Descripción

Central Nervous System Involvement

Tipo de datos

boolean

Alias
UMLS CUI [1]
C4050309
positive for hiv
Descripción

HIV Seropositivity

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0019699
who performance index 3 or 4
Descripción

WHO performance status scale

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1298650
secondary malignoma
Descripción

Secondary Neoplasm

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2939419
concurrent disease that prohibits chemotherapy
Descripción

Comorbidity Preventing Chemotherapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C1292733
UMLS CUI [1,3]
C0392920
known hypersensitivity towards the study interventions or their constituents
Descripción

Hypersensitivity Intervention Investigational | Hypersensitivity Component Intervention Investigational

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0184661
UMLS CUI [1,3]
C1517586
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C1705248
UMLS CUI [2,3]
C0184661
UMLS CUI [2,4]
C1517586
neutropenia or thrombopenia
Descripción

Neutropenia | Thrombocytopenia

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0027947
UMLS CUI [2]
C0040034
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Similar models

Eligibility Diffuse Large B-Cell Lymphoma NCT00575406

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Diffuse Large B-Cell Lymphoma CD20 antigen positive
Item
histologically confirmed, cd20 positive, diffuse large b-cell lymphoma (dlcl)
boolean
C0079744 (UMLS CUI [1,1])
C3888518 (UMLS CUI [1,2])
Measurable Disease
Item
measurable disease according to international criteria
boolean
C1513041 (UMLS CUI [1])
Gender
Item
male or female
boolean
C0079399 (UMLS CUI [1])
Age
Item
age 18 years and above
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Myocardial Infarction
Item
myocardial infarction within 6 months prior to study entry
boolean
C0027051 (UMLS CUI [1])
Heart failure New York Heart Association Classification
Item
cardiac insufficiency nyha grade 3 or 4
boolean
C0018801 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
Chemotherapy | Therapeutic radiology procedure
Item
previous treatment with chemotherapy or radiotherapy
boolean
C0392920 (UMLS CUI [1])
C1522449 (UMLS CUI [2])
Central Nervous System Involvement
Item
cns involvement of the disease
boolean
C4050309 (UMLS CUI [1])
HIV Seropositivity
Item
positive for hiv
boolean
C0019699 (UMLS CUI [1])
WHO performance status scale
Item
who performance index 3 or 4
boolean
C1298650 (UMLS CUI [1])
Secondary Neoplasm
Item
secondary malignoma
boolean
C2939419 (UMLS CUI [1])
Comorbidity Preventing Chemotherapy
Item
concurrent disease that prohibits chemotherapy
boolean
C0009488 (UMLS CUI [1,1])
C1292733 (UMLS CUI [1,2])
C0392920 (UMLS CUI [1,3])
Hypersensitivity Intervention Investigational | Hypersensitivity Component Intervention Investigational
Item
known hypersensitivity towards the study interventions or their constituents
boolean
C0020517 (UMLS CUI [1,1])
C0184661 (UMLS CUI [1,2])
C1517586 (UMLS CUI [1,3])
C0020517 (UMLS CUI [2,1])
C1705248 (UMLS CUI [2,2])
C0184661 (UMLS CUI [2,3])
C1517586 (UMLS CUI [2,4])
Neutropenia | Thrombocytopenia
Item
neutropenia or thrombopenia
boolean
C0027947 (UMLS CUI [1])
C0040034 (UMLS CUI [2])
Volver a la parte superior de la página 

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